2-METHYLINDOL

AlkaPlorer ID: AK004571

Synonym: '2-Methylindole'

IUPAC Name: 2-methyl-1H-indole

Structure

SMILES: CC1=CC2=CC=CC=C2N1

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InChI: InChI=1S/C9H9N/c1-7-6-8-4-2-3-5-9(8)10-7/h2-6,10H,1H3

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InChIKey: BHNHHSOHWZKFOX-UHFFFAOYSA-N

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Reference

PubChem CID: 7224

CAS: 90-25-5

LOTUS: LTS0190864

COCONUT: CNP0223946

Source

Species Genus Family Order Class Phylum Kingdom Domain
None None Streptomycetaceae Kitasatosporales Actinomycetes Actinomycetota None Bacteria

Properties Information

Molecule Weight: 131.17799999999997

TPSA: 15.79

MolLogP: 2.4763200000000003

Number of H-Donors: 1

Number of H-Acceptors: 0

RingCount: 2

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Electrophorus electricus Acetylcholinesterase Inhibition 17.97 % 10.1016/j.bmcl.2012.02.057
Homo sapiens Androgen Receptor Inhibition 16.0 % 10.1073/pnas.0708036104
Homo sapiens PI3-kinase p110-alpha/p85-alpha Inhibition 25.0 % 10.1016/j.bmc.2017.01.012
Homo sapiens PI3-kinase p110-alpha subunit Inhibition 25.0 % 10.1016/j.bmc.2017.01.012
Rattus norvegicus Rattus norvegicus Inhibition nan % 10.1021/jm00214a015
None Calvarial osteoblast Activity nan None 10.1016/j.ejmech.2022.114813

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT012880 C[C@@H](O)[C@H](N)C(=O)O.Cc1cc2ccccc2[nH]1>>Cc1[nH]c2ccccc2c1[C@H](C)[C@H](N)C(=O)O enzymemap_83788
AKRT014974 Cc1cc2ccccc2[nH]1.N[C@@H](CO)C(=O)O>>Cc1[nH]c2ccccc2c1C[C@H](N)C(=O)O enzymemap_84072
AKRT014975 Cc1cc2ccccc2[nH]1.O=C=O>>Cc1[nH]c2ccccc2c1C(=O)O enzymemap_82182